COMPLETED

Opioid Rapid Response System: Naloxone Training in Communities

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The pervasive impact of the opioid epidemic has touched all layers of society for the past two decades, resulting in over 115 deaths daily and imposing annual costs of $78.5 billion. Responding swiftly to overdoses, akin to various medical emergencies, poses a significant challenge, particularly in geographically dispersed rural areas and densely populated urban settings. Effectively delivering the life-saving drug naloxone, which counteracts the effects of overdoses, necessitates a well-coordinated and cost-efficient response system. Simply opting for widespread distribution of naloxone, even with citizen involvement, proves to be a financially burdensome approach when compared to more targeted strategies. Moreover, obstacles such as limited access, inadequate or unavailable naloxone training, and delayed response times from emergency responders compound the problem. Addressing these issues, the proposed Opioid Rapid Response System (ORRS) project seeks to advance prevention science by adopting an innovative approach that incorporates technology and contemporary communication theory. The primary objective of the ORRS project is to mitigate opioid overdose deaths by enlisting and training citizens to administer naloxone in response to such events. Leveraging the PulsePoint health app, which connects citizens to cardiac events, the ORRS project will extend its capabilities to respond to overdose incidents. This initiative involves comprehensive development of ORRS, followed by a randomized clinical trial on a national scale to assess its effectiveness. The study aims to contribute to both prevention and implementation science by identifying optimal recruitment strategies and testing a model of online training. In pursuit of these objectives, the study is guided by the following Specific Aims: SA 1: Refine and complete the development of ORRS. SA 2: Conduct a randomized clinical trial to evaluate the effectiveness of the intervention. SA 3: Prepare ORRS for dissemination.

Official Title

Developing and Testing the Opioid Rapid Response System

Quick Facts

Study Start:2024-05-24
Study Completion:2025-12-29
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06238128

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Citizens who live in participating PulsePoint communities
  2. * Must to be 18 and older
  3. * Must be fluent in English
  4. * Must have access to the mobile data and able to download and use apps in a smartphone
  1. * Citizens who do not live in participating PulsePoint communities
  2. * Under 18-year-old
  3. * Citizens who are not fluent in English
  4. * Citizens who do not have access to mobile data and unable to download and use apps in a smartphone.

Contacts and Locations

Principal Investigator

Hye Jeong Choi
PRINCIPAL_INVESTIGATOR
Univeristy of Missouri
Michael Hecht
PRINCIPAL_INVESTIGATOR
Real Prevention

Study Locations (Sites)

Ewald & Wasserman Research Consultants, LLC
San Francisco, California, 94104
United States

Collaborators and Investigators

Sponsor: University of Missouri-Columbia

  • Hye Jeong Choi, PRINCIPAL_INVESTIGATOR, Univeristy of Missouri
  • Michael Hecht, PRINCIPAL_INVESTIGATOR, Real Prevention

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-05-24
Study Completion Date2025-12-29

Study Record Updates

Study Start Date2024-05-24
Study Completion Date2025-12-29

Terms related to this study

Keywords Provided by Researchers

  • naloxone training
  • Community-engagement

Additional Relevant MeSH Terms

  • Opioid Overdose